Differential propagation of ripples along the proximodistal and septotemporal axes of dorsal CA1 of rats
The functional connectivity of the hippocampus with its primary cortical input, the entorhinal cortex, is organized topographically. In area CA1 of the hippocampus, this leads to different functional gradients along the proximodistal and septotemporal axes of spatial/sensory responsivity and spatial...
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Veröffentlicht in: | Hippocampus 2020-09, Vol.30 (9), p.970-986 |
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description | The functional connectivity of the hippocampus with its primary cortical input, the entorhinal cortex, is organized topographically. In area CA1 of the hippocampus, this leads to different functional gradients along the proximodistal and septotemporal axes of spatial/sensory responsivity and spatial resolution respectively. CA1 ripples, a network phenomenon, allow us to test whether the hippocampal neural network shows corresponding gradients in functional connectivity along the two axes. We studied the occurrence and propagation of ripples across the entire proximodistal axis along with a comparable spatial range of the septotemporal axis of dorsal CA1. We observed that ripples could occur at any location, and their amplitudes were independent of the tetrode location along the proximodistal and septotemporal axes. When a ripple was detected on a particular tetrode (“reference tetrode”), however, the probability of cooccurrence of ripples and ripple amplitude observed on the other tetrodes decreased as a function of distance from the reference tetrode. This reduction was greater along the proximodistal axis than the septotemporal axis. Furthermore, we found that ripples propagate primarily along the proximodistal axis. Thus, over a spatial scale of ∼1.5 mm, the network is anisotropic along the two axes, complementing the topographically organized cortico‐hippocampal connections. |
doi_str_mv | 10.1002/hipo.23211 |
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In area CA1 of the hippocampus, this leads to different functional gradients along the proximodistal and septotemporal axes of spatial/sensory responsivity and spatial resolution respectively. CA1 ripples, a network phenomenon, allow us to test whether the hippocampal neural network shows corresponding gradients in functional connectivity along the two axes. We studied the occurrence and propagation of ripples across the entire proximodistal axis along with a comparable spatial range of the septotemporal axis of dorsal CA1. We observed that ripples could occur at any location, and their amplitudes were independent of the tetrode location along the proximodistal and septotemporal axes. When a ripple was detected on a particular tetrode (“reference tetrode”), however, the probability of cooccurrence of ripples and ripple amplitude observed on the other tetrodes decreased as a function of distance from the reference tetrode. This reduction was greater along the proximodistal axis than the septotemporal axis. Furthermore, we found that ripples propagate primarily along the proximodistal axis. 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In area CA1 of the hippocampus, this leads to different functional gradients along the proximodistal and septotemporal axes of spatial/sensory responsivity and spatial resolution respectively. CA1 ripples, a network phenomenon, allow us to test whether the hippocampal neural network shows corresponding gradients in functional connectivity along the two axes. We studied the occurrence and propagation of ripples across the entire proximodistal axis along with a comparable spatial range of the septotemporal axis of dorsal CA1. We observed that ripples could occur at any location, and their amplitudes were independent of the tetrode location along the proximodistal and septotemporal axes. When a ripple was detected on a particular tetrode (“reference tetrode”), however, the probability of cooccurrence of ripples and ripple amplitude observed on the other tetrodes decreased as a function of distance from the reference tetrode. This reduction was greater along the proximodistal axis than the septotemporal axis. Furthermore, we found that ripples propagate primarily along the proximodistal axis. Thus, over a spatial scale of ∼1.5 mm, the network is anisotropic along the two axes, complementing the topographically organized cortico‐hippocampal connections.</description><subject>Cortex (entorhinal)</subject><subject>Cortex (somatosensory)</subject><subject>Hippocampus</subject><subject>lateral Entorhinal cortex (LEC)</subject><subject>medial Entorhinal cortex (MEC)</subject><subject>Neural networks</subject><subject>proximodistal (transverse) axis</subject><subject>ripples</subject><subject>septotemporal (longitudinal) axis</subject><subject>Spatial discrimination</subject><issn>1050-9631</issn><issn>1098-1063</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2020</creationdate><recordtype>article</recordtype><recordid>eNp90E9LwzAYBvAgipvTix9ACl5E6Mybt03b45h_JgzmQc8la5Mto21q0qF-e9NtevDgKcnLLw8vDyGXQMdAKbtb69aMGTKAIzIEmqUhUI7H_T2mYcYRBuTMuQ2lADGlp2SADFPOEj4k63utlLSy6bSogtaaVqxEp00TGBVY3baVdIGoTLMKurXswaeuTald57loysDJtjOdrFtj-8mn5_5naazzz-kEdjmic-fkRInKyYvDOSJvjw-v01k4Xzw9TyfzsMAMIUwERlJlCrjwyxZcYUIhozEv4wiFQiVZJpEtlwnGPGIijkRJOU9TlqkoKlIckZt9rl_1fStdl9faFbKqRCPN1uUsojSGKEt6ev2HbszWNn47r5AjIqSJV7d7VVjjnJUqb62uhf3KgeZ9_3nff77r3-OrQ-R2Wcvyl_4U7gHswYeu5Nc_Ufns-WWxD_0G5jGPVg</recordid><startdate>202009</startdate><enddate>202009</enddate><creator>Kumar, Mekhala</creator><creator>Deshmukh, Sachin S.</creator><general>John Wiley & Sons, Inc</general><general>Wiley Subscription Services, Inc</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7QG</scope><scope>7TK</scope><scope>K9.</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0002-9395-0376</orcidid><orcidid>https://orcid.org/0000-0002-8421-4158</orcidid></search><sort><creationdate>202009</creationdate><title>Differential propagation of ripples along the proximodistal and septotemporal axes of dorsal CA1 of rats</title><author>Kumar, Mekhala ; Deshmukh, Sachin S.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3931-7a34ef9f16a115c6f37019056d543af3fe29e32bb735642a54ad0668829f44c83</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2020</creationdate><topic>Cortex (entorhinal)</topic><topic>Cortex (somatosensory)</topic><topic>Hippocampus</topic><topic>lateral Entorhinal cortex (LEC)</topic><topic>medial Entorhinal cortex (MEC)</topic><topic>Neural networks</topic><topic>proximodistal (transverse) axis</topic><topic>ripples</topic><topic>septotemporal (longitudinal) axis</topic><topic>Spatial discrimination</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Kumar, Mekhala</creatorcontrib><creatorcontrib>Deshmukh, Sachin S.</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>Animal Behavior Abstracts</collection><collection>Neurosciences Abstracts</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>MEDLINE - Academic</collection><jtitle>Hippocampus</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Kumar, Mekhala</au><au>Deshmukh, Sachin S.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Differential propagation of ripples along the proximodistal and septotemporal axes of dorsal CA1 of rats</atitle><jtitle>Hippocampus</jtitle><addtitle>Hippocampus</addtitle><date>2020-09</date><risdate>2020</risdate><volume>30</volume><issue>9</issue><spage>970</spage><epage>986</epage><pages>970-986</pages><issn>1050-9631</issn><eissn>1098-1063</eissn><abstract>The functional connectivity of the hippocampus with its primary cortical input, the entorhinal cortex, is organized topographically. In area CA1 of the hippocampus, this leads to different functional gradients along the proximodistal and septotemporal axes of spatial/sensory responsivity and spatial resolution respectively. CA1 ripples, a network phenomenon, allow us to test whether the hippocampal neural network shows corresponding gradients in functional connectivity along the two axes. We studied the occurrence and propagation of ripples across the entire proximodistal axis along with a comparable spatial range of the septotemporal axis of dorsal CA1. We observed that ripples could occur at any location, and their amplitudes were independent of the tetrode location along the proximodistal and septotemporal axes. When a ripple was detected on a particular tetrode (“reference tetrode”), however, the probability of cooccurrence of ripples and ripple amplitude observed on the other tetrodes decreased as a function of distance from the reference tetrode. 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subjects | Cortex (entorhinal) Cortex (somatosensory) Hippocampus lateral Entorhinal cortex (LEC) medial Entorhinal cortex (MEC) Neural networks proximodistal (transverse) axis ripples septotemporal (longitudinal) axis Spatial discrimination |
title | Differential propagation of ripples along the proximodistal and septotemporal axes of dorsal CA1 of rats |
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